Related Experiment Video
Updated: Jan 9, 2026

10:03
Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
26.0K
Synergistic Zn/Al Co-Doping and Sodium Enrichment Enable Reversible Phase Transitions in High-Performance Layered
Yaru Qin1,2, Tingfei Yang1,3, Na Chen3
1School of Chemistry and Materials Science, Qinghai Minzu University, Xining 810007, China.
Molecules (Basel, Switzerland)
|December 11, 2025
Summary
This study enhances sodium-ion battery cathodes by co-doping with Zn/Al and enriching sodium. The new material shows improved stability and performance, overcoming capacity fade issues for practical applications.
Area of Science:
- Materials Science
- Electrochemistry
- Energy Storage
Background:
- Layered transition-metal oxides are promising sodium-ion battery cathodes.
- Prototypical P2-Na0.67Ni0.33Mn0.67O2 (NM) suffers from irreversible phase transitions and capacity fade at high voltages.
Purpose of the Study:
- To develop a cooperative regulation strategy for enhancing the stability and performance of sodium-ion battery cathodes.
- To synthesize and characterize a novel P2-Na0.80Ni0.14Zn0.14Mn0.58Al0.14O2 (NMZA-N14) material.
Main Methods:
- Cooperative regulation strategy involving Zn/Al co-doping and Na enrichment.
- Synthesis of P2-Na0.80Ni0.14Zn0.14Mn0.58Al0.14O2 (NMZA-N14).
- Electrochemical performance testing (cycling, rate capability), kinetic analysis, and in situ X-ray diffraction.
Main Results:
- NMZA-N14 exhibits high initial discharge capacity (125 mAh g-1 at 0.1C) and excellent cycling stability (98.6% capacity retention after 100 cycles at 0.2C).
- Improved Na+ diffusion coefficient and lower charge-transfer resistance indicate accelerated ion transport.
- In situ XRD confirms a reversible P2 → OP4 phase transition with minimal volume change (~2.27%), preventing structural degradation.
Conclusions:
- Synergistic modulation via Zn/Al co-doping and Na enrichment significantly enhances structural stability and electrochemical kinetics.
- The developed NMZA-N14 material offers a viable pathway for designing high-performance sodium-ion battery cathodes.
- This strategy effectively suppresses irreversible phase transitions and capacity fade in layered transition-metal oxides.
More Related Videos
Related Concept Videos
Formation of Complex Ions
25.6K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
25.6K
Ionic Strength: Effects on Chemical Equilibria
2.5K
The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary...
In this solution, the primary...
2.5K
Electrolysis
30.0K
In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
30.0K
Electrodeposition
1.2K
Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
Electrodeposition can...
Electrodeposition can...
1.2K
Ion Exchange
1.1K
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
1.1K
Qualitative Analysis
23.6K
For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
For instance, group IV...
23.6K

